Kiew Lik Voon, Munavvar Abdul Sattar, Law Chung Hiong, Azizan Abdullah Nor, Nazarina Abdul Rahman, Sidik Khalifah, Johns Edward J
Department of Pharmaceutical Sciences, University of Science Malaysia, Penang, Malaysia.
J Physiol. 2004 Jun 15;557(Pt 3):981-9. doi: 10.1113/jphysiol.2004.061788. Epub 2004 Mar 26.
An antisense oligodeoxynucleotide (As-ODN) to the 3' untranslated region of the mRNA sequence expressing the intracellular adhesion molecule-1 (ICAM-1) was employed to determine ICAM-1's role in renal ischaemia-reperfusion injury in the rat. Wistar-Kyoto rats receiving i.v. either lipofectin-As-ODN (As-ODN group), lipofectin-reverse ODN (Rv-ODN group) or lipofectin (ischaemia control group) 8 h prior to study were anaesthetized and subjected to 30 min of renal artery occlusion. Renal haemodynamic and excretory parameters were monitored before and after renal ischaemia. On termination of the study renal tissue was subjected to histological and Western blot analysis. Renal blood flow decreased in the 3 h post-ischaemia period in the ischaemia control and Rv-ODN groups, but was maintained in the As-ODN group. Glomerular filtration rate was depressed initially but gradually increased to 10% above basal levels in the ischaemia control and Rv-ODN groups, but was below basal levels (20%) in the As-ODN group. There was a three- to fourfold increase in sodium and water excretion following ischaemia in the ischaemia control and reverse-ODN groups but not in the As-ODN treated group. The As-ODN ameliorated the histological evidence of ischaemic damage and reduced ICAM-1 protein levels to a greater extent in the medulla than cortex. These observations suggested that in the post-ischaemic period afferent and efferent arteriolar tone was increased with a loss of reabsorptive capacity which was in part due to ICAM-1. The possibility arises that the action of ICAM-1 at vascular and tubular sites in the deeper regions of the kidney contributes to the ischaemia-reperfusion injury.
采用针对表达细胞间黏附分子 -1(ICAM -1)的mRNA序列3'非翻译区的反义寡脱氧核苷酸(As -ODN),以确定ICAM -1在大鼠肾缺血再灌注损伤中的作用。在研究前8小时经静脉注射脂质体 -As -ODN(As -ODN组)、脂质体 -反义寡核苷酸(Rv -ODN组)或脂质体(缺血对照组)的Wistar -Kyoto大鼠被麻醉,并接受30分钟的肾动脉阻断。在肾缺血前后监测肾血流动力学和排泄参数。研究结束时,对肾组织进行组织学和蛋白质印迹分析。缺血对照组和Rv -ODN组在缺血后3小时肾血流量下降,但As -ODN组血流量得以维持。缺血对照组和Rv -ODN组肾小球滤过率最初降低,但逐渐增加至基础水平以上10%,而As -ODN组则低于基础水平(20%)。缺血对照组和反义寡核苷酸组缺血后钠和水排泄增加了三到四倍,但As -ODN处理组未出现这种情况。As -ODN改善了缺血损伤的组织学证据,并在髓质中比皮质更大程度地降低了ICAM -1蛋白水平。这些观察结果表明,在缺血后时期,入球和出球小动脉张力增加,重吸收能力丧失,部分原因是ICAM -1。有可能ICAM -1在肾深部区域的血管和肾小管部位的作用促成了缺血再灌注损伤。